Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Qiumei Du"'
Autor:
Pratibha Bhalla, Qiumei Du, Ashwani Kumar, Chao Xing, Angela Moses, Igor Dozmorov, Christian A. Wysocki, Ondine B. Cleaver, Timothy J. Pirolli, Mary Louise Markert, Maria Teresa de la Morena, Antonio Baldini, Nicolai S.C. van Oers
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 13 (2023)
Externí odkaz:
https://doaj.org/article/146af13047684647a7ef352bc9881ac0
Publikováno v:
Frontiers in Genetics, Vol 10 (2020)
Chromosome 22q11.2 deletion syndrome (22q11.2del) is a complex, multi-organ disorder noted for its varying severity and penetrance among those affected. The clinical problems comprise congenital malformations; cardiac problems including outflow tract
Externí odkaz:
https://doaj.org/article/a08679cba340473f9ae0392ac7cf4a0a
Autor:
Jingyun Li, Qiumei Du, Rui Hu, Yanbing Wang, Xiangyun Yin, Haisheng Yu, Peishuang Du, Joël Plumas, Laurence Chaperot, Yong-jun Liu, Liguo Zhang
Publikováno v:
Protein & Cell, Vol 7, Iss 4, Pp 291-294 (2016)
Externí odkaz:
https://doaj.org/article/cdaee0cf3e624354990c253f61d07b92
Autor:
Yuhua Wang, Qiumei Du, Hongjie Pan, Geetika Bajpai, Tao Liu, Jason Noon, Yao Lu, Jinqiu He, Yan Li, Qingfang Chen, Yongqiang Wang, Xingxing Jia, Fei Chen, Youhong Wang, Yiping Rong, Yun He, Joe Zhao, Musheng Bao
Publikováno v:
Regular and Young Investigator Award Abstracts.
Autor:
Pratibha Bhalla, Qiumei Du, Ashwani Kumar, Chao Xing, Angela Moses, Igor Dozmorov, Christian A. Wysocki, Ondine B. Cleaver, Timothy J. Pirolli, Mary Louise Markert, Maria Teresa de la Morena, Antonio Baldini, Nicolai S.C. van Oers
Publikováno v:
The Journal of clinical investigation. 132(22)
22q11.2 deletion syndrome (22q11.2DS) is the most common human chromosomal microdeletion, causing developmentally linked congenital malformations, thymic hypoplasia, hypoparathyroidism, and/or cardiac defects. Thymic hypoplasia leads to T cell lympho
Autor:
Bhalla, Pratibha1, Qiumei Du1, Kumar, Ashwani2, Chao Xing2,3,4, Moses, Angela1, Dozmorov, Igor1, Wysocki, Christian A.5,6, Cleaver, Ondine B.7, Pirolli, Timothy J.8, Markert, Mary Louise9, de la Morena, Maria Teresa10, Baldini, Antonio11, van Oers, Nicolai S. C.1,5,12 Nicolai.vanoers@utsouthwestern.edu
Publikováno v:
Journal of Clinical Investigation. 11/15/2022, Vol. 132 Issue 22, p1-17. 17p.
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 10 (2020)
Frontiers in Genetics, Vol 10 (2020)
Chromosome 22q11.2 deletion syndrome (22q11.2del) is a complex, multi-organ disorder noted for its varying severity and penetrance among those affected. The clinical problems comprise congenital malformations; cardiac problems including outflow tract
Autor:
Yanbing Wang, Rui Hu, Yong-Jun Liu, Peishuang Du, Xiangyun Yin, Joel Plumas, Laurence Chaperot, Qiumei Du, Haisheng Yu, Liguo Zhang, Jingyun Li
Publikováno v:
Protein & Cell, Vol 7, Iss 4, Pp 291-294 (2016)
Protein & Cell
Protein & Cell
Dear Editor, Plasmacytoid dendritic cells (pDCs) are the professional type I interferon-producing cells of the immune system, which rapidly produce massive amounts of type I interferons (IFN-I) in response to viruses or other nucleic acids ligands th
Publikováno v:
Cancer Research. 80:6056-6056
CD73, an ecto-5'-nucleotidase, plays a major role in de-phosphorylation of the extracellular adenosine monophosphate (AMP) to adenosine, which in turn is a potent immunosuppressive metabolite that modulates the immune reaction within the tumor microe
Autor:
Maria Teresa de la Morena, Ashley R. Hoover, Tsung Cheng Chang, Qiumei Du, Erika Molina, Ondine Cleaver, Shaheen Khan, Joshua T. Mendell, Igor Dozmorov, Prithvi Raj, Nicolai S. C. van Oers
Publikováno v:
Dev Cell
Summary MicroRNAs (miRNAs) are processed from primary miRNA transcripts (pri-miRNAs), many of which are annotated as long noncoding RNAs (lncRNAs). We assessed whether MIR205HG, the host gene for miR-205, has independent functions as an lncRNA. Compa